HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096202Generated: November 1, 2026
Sodium Bicarbonate → 1-(3,4-Dichloro-phenyl)-4-[(S)-3-((S)-4-hydroxy-6-aza-spiro[2.5]oct-6-yl)-1-hydroxymethyl-propyl]-[1,4]diazepan-5-one
https://huagongshe.com/reaction/1096202
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | (S)-2-[4-(3,4-Dichloro-phenyl)-7-oxo-[1,4]diazepan-1-yl]-4-((S)-4-hydroxy-6-aza-spiro[2.5]oct-6-yl)-butyric Acid methyl ester | HCID 59159299 | — |
| Product | 1-(3,4-Dichloro-phenyl)-4-[(S)-3-((S)-4-hydroxy-6-aza-spiro[2.5]oct-6-yl)-1-hydroxymethyl-propyl]-[1,4]diazepan-5-one | HCID 45100715 | 75.2% |
Reaction Steps
A solution of 0.180 g (0.37 mmol) of (S)-2-[4-(3,4-dichloro-phenyl)-7-oxo-[1,4]diazepan-1-yl]-4-((S)-4-hydroxy-6-aza-spiro[2.5]oct-6-yl)-butyric acid methyl ester in 4 ml of ETOH was treated at 0° C. with 0.017 g (0.74 mmol) of LiBH4. The reaction was stirred 10 min at 0° C. and 22 h at RT, cooled (0° C.) and treated with 0.009 g (0.37 mmol) of LiBH4 and after 5 h again cooled (0° C.) and treated with 0.009 g (0.37 mmol) of LiBH4. After 1 h at RT, the reaction was cooled (0° C.), acidified with 10% aq. KHSO4 solution and then basified with sat. aq NaHCO3 solution and extracted with EtOAc (3×). The organic phases were washed with aq. 10% NaCl solution, dried over Na2SO4 evaporated and purified by flash silica gel column (CH2Cl2:MeOH 95:5 to 9:1) to yield 0.127 g (75%) of the title compound as white foam. MS: 456.2 (MH+, 2Cl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138175B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-185aa2e7285c45f493c35af05996952c |
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| Source note | uspto-grants-2012_03 |
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