HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,5-Dimethyl-4-Isoxazolecarbaldehyde → HCID 58055071, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,5-Dimethyl-4-Isoxazolecarbaldehyde | HCID 289576 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86661313 | HCID 86661313 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 58055071 | HCID 58055071 | — |
Reaction Steps
NaBH4 (35 mg, 1 mmol) was added in portions to a MeOH (5 mL) solution of 3,5-dimethylisoxazole-4-carbaldehyde (65 mg, 0.5 mmol) and 1-(4-(aminomethyl) thiazol-2-yl)-3-(3-fluorobenzyl)urea hydrochloride (157 mg, 0.5 mmol) at 0 C. The mixture was stirred for 6 hours then quenched with dilute HCl solution. Basic aqueous work-up with CH2Cl2 followed by flash chromatography afforded Intermediate 61: 1-(4-(((3,5-dimethylisoxazol-4-yl)methylamino)methyl)thiazol-2-yl)-3-(3-fluorobenzyl)urea. 1H NMR (400 MHz, CDCl3): δ 8.2 (1H, br), 7.27 (m, 1H), 6.92 (m, 3H), 6.60 (s, 1H), 4.37 (d, 2H), 3.66 (s, 2H), 3.33 (s, 2H), 2.22 (s, 3H), 2.11 (s, 3H). MS (ES+): M/Z 390 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08148380B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-8e2bc4bdb53c41399610250f3cee2fa4 |
| Source note | uspto-grants-2012_04 |