Hydrochloric Acid → HCID 86692135, compound
Reaction equation
[N:1]1[C:6]2[NH:7][CH:8]=[CH:9][C:5]=2[C:4]([N:10]2[CH2:14][CH2:13][C@@H:12]([NH:15]C(=O)OC(C)(C)C)[CH2:11]2)=[N:3][CH:2]=1.[ClH:23]>>[ClH:23].[N:1]1[C:6]2[NH:7][CH:8]=[CH:9][C:5]=2[C:4]([N:10]2[CH2:14][CH2:13][C@@H:12]([NH2:15])[CH2:11]2)=[N:3][CH:2]=1Participants
3
Procedure
(R)-tert-butyl 1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrrolidin-3-ylcarbamate (600 mg, 1.97 mmol) was treated with HCl (in MeOH, 6 N, 5 mL) at the ambient temperature for 2 h. The volatiles were removed under reduced pressure to give (R)-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrrolidin-3-amine hydrochloride salt. MS (m/z): 204 (M+H)+.
Workup
- customThe volatiles were removed under reduced pressure
Sources & evidence
- ORD record
- ord-36ac951c99cc4c90bb4988350fc2902e
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09346810B2
Reaction notes
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