HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177408Generated: October 30, 2026
Acetic Acid → Methyl 1-((4-(5-chlorothiazolo[5,4-b]pyridine-2-yl)-3-fluorophenyl)methyl)azetidine-3-carboxylate
https://huagongshe.com/reaction/1177408
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Methyl azetidine-3-carboxylate hydrochloride | HCID 21100040 | — |
| Reactant | 4-(5-Chlorothiazolo[5,4-b]pyridine-2-yl)-3-fluorobenzaldehyde | HCID 86638706 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 1-((4-(5-chlorothiazolo[5,4-b]pyridine-2-yl)-3-fluorophenyl)methyl)azetidine-3-carboxylate | HCID 86638707 | — |
Reaction Steps
A mixture of 4-(5-chlorothiazolo[5,4-b]pyridine-2-yl)-3-fluorobenzaldehyde (2.08 g, 7.11 mmol), methyl azetidine-3-carboxylate hydrochloride (1.62 g, 10.7 mmol), N-ethyl-N-isopropylpropan-2-amine (1.86 mL, 10.7 mmol) in dichloromethane (40.00 mL) and methanol (30.00 mL) was stirred for 5 min. Then acetic acid (1.64 mL, 28.4 mmol) was added and the mixture was allowed to stir for 90 min at 50° C. Sodium cyanoborohydride (0.223 g, 3.55 mmol) was added. After 15 min, the solvent removed, and the mixture concentrated onto silica gel. Purification by silica gel chromatography, 120 g column, 30-40% EtOAc/hex followed by 50-60% (3% TEA in EtOAc/hex) gave methyl 1-((4-(5-chlorothiazolo[5,4-b]pyridine-2-yl)-3-fluorophenyl)methyl)azetidine-3-carboxylate. MS (ESI) m/z: calculated: 391.1; Observed: 392.0 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842685B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-5b21c1c25c3c4b72b0cd46b965e1cf2f |
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| Source note | uspto-grants-2010_11 |
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